205114-66-5 Usage
Description
(2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid is a complex chiral molecule with a unique molecular structure that features a benzyl group, hydroxy groups, a butanedioic acid group, a prop-2-enoyl group, and a methoxyphenyl group. The presence of two asymmetric carbon atoms, denoted as 2R and 3S, contributes to its distinct stereochemistry. (2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid holds promise for various applications in pharmaceuticals, biochemistry, and organic chemistry due to its intricate and specific structural features, which are likely to confer particular biological and chemical properties.
Uses
Used in Pharmaceutical Industry:
(2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid is used as a pharmaceutical agent for its potential therapeutic effects. (2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid's complex structure, which includes multiple functional groups, suggests that it may interact with biological targets in specific ways, leading to possible applications in the treatment of various diseases.
Used in Biochemical Research:
In the field of biochemistry, (2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid serves as a valuable research tool. Its unique stereochemistry and functional groups make it an interesting subject for studying enzyme interactions, metabolic pathways, and the development of novel biochemical assays.
Used in Organic Chemistry:
(2R,3S)-2-(3,4-dihydroxybenzyl)-2-hydroxy-3-[(2E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxybutanedioic acid is utilized in organic chemistry for the synthesis of complex organic compounds and the exploration of novel chemical reactions. Its specific structure allows for targeted functionalization and the creation of new molecules with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 205114-66-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,1,1 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 205114-66:
(8*2)+(7*0)+(6*5)+(5*1)+(4*1)+(3*4)+(2*6)+(1*6)=85
85 % 10 = 5
So 205114-66-5 is a valid CAS Registry Number.